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Synthesis and in vitro bioactivity of CaO-SiO2-P2O5 mesoporous microspheres

机译:CaO-SiO2-P2O5介孔微球的合成及体外生物活性

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摘要

In CaO-SiO2-P2O5 system, mesoporous bioactive microspheres with comparatively high P2O5 content (5 mol%-15 mol%) were successfully synthesized by co-templates of non-ionic block copolymer EO_(20)-PO_(70)-EO_(20) (P123) and cationic surfactant cetyltrimethylammonium bromide (CTAB), followed by hydro-thermal and calcination treatment. The structural, morphological and textural properties were investigated by small-angle X-ray diffraction (SAXRD), transmission electron microscope (TEM), scanning electron microscope (SEM), Fourier-transform infrared (FT1R) spectroscope and N2 sorption/desorption techniques. Results showed that the obtained microspheres with a diameter of ~5 um exhibit hexagonal ordered and wormlike mesostructures with certain uniformity in size and morphology. This material has BJH pore size of ~7.3 nm and BET specific surface area of ~618 m2/g. Samples with 15 mol% P2O5 induce apatite formation on their surface after soaked in simulated body fluid (SBF) solution for 7 d. The bioactive mesoporous microspheres could be used as a drug carrier for bone repair in future.
机译:在CaO-SiO2-P2O5体系中,通过非离子嵌段共聚物EO_(20)-PO_(70)-EO_()的共模板成功合成了P2O5含量较高(5 mol%-15 mol%)的中孔生物活性微球。 20)(P123)和阳离子表面活性剂溴化十六烷基三甲基铵(CTAB),然后进行水热和煅烧处理。通过小角度X射线衍射(SAXRD),透射电子显微镜(TEM),扫描电子显微镜(SEM),傅立叶变换红外光谱仪(FT1R)和N2吸附/解吸技术研究了结构,形态和织构特性。结果表明,所获得的直径约5μm的微球呈现出六角形的有序和蠕虫状的介孔结构,在尺寸和形态上具有一定的一致性。该材料的BJH孔径约为7.3 nm,BET比表面积约为618 m2 / g。含15 mol%P2O5的样品在模拟体液(SBF)溶液中浸泡7 d后,在其表面上诱导形成磷灰石。具有生物活性的中孔微球体将​​来可以用作骨修复的药物载体。

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